Variant report
Variant | rs10961064 |
---|---|
Chromosome Location | chr9:13465860-13465861 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10114185 | 1.00[AFR][1000 genomes] |
rs10119562 | 0.83[AFR][1000 genomes] |
rs10120898 | 0.91[AFR][1000 genomes] |
rs10124485 | 0.83[AFR][1000 genomes] |
rs10961060 | 1.00[AFR][1000 genomes] |
rs10961061 | 1.00[AFR][1000 genomes] |
rs10961062 | 1.00[AFR][1000 genomes] |
rs10961063 | 0.91[AFR][1000 genomes] |
rs10961066 | 1.00[AFR][1000 genomes] |
rs10961067 | 1.00[AFR][1000 genomes] |
rs11506362 | 1.00[AFR][1000 genomes] |
rs12341780 | 1.00[AFR][1000 genomes] |
rs12353374 | 1.00[AFR][1000 genomes] |
rs13440025 | 1.00[AFR][1000 genomes] |
rs13440030 | 1.00[AFR][1000 genomes] |
rs13440033 | 1.00[AFR][1000 genomes] |
rs13440173 | 1.00[AFR][1000 genomes] |
rs13440328 | 1.00[AFR][1000 genomes] |
rs73412169 | 1.00[AFR][1000 genomes] |
rs73412170 | 1.00[AFR][1000 genomes] |
rs73412172 | 1.00[AFR][1000 genomes] |
rs73412173 | 1.00[AFR][1000 genomes] |
rs73414120 | 1.00[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv892578 | chr9:12942956-13485035 | Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
2 | nsv831515 | chr9:13333205-13517308 | Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:13456000-13467400 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |